prescribing algorithms and pharmacotherapy troubleshooting ... · •cough develops pharmacological...
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BASED ON ENHANCING KNOWLEDGE FOR INTERPROFESSIONAL CARE IN HEART FAILURE (EKWIP-HF) INTERVENTION (HECKMAN ET AL, 2017).
©2019, GEORGE A. HECKMAN, LORA BRUYN-MARTIN , SCHLEGEL-UW RESEARCH INSTITUTE FOR AGING, AND SCHLEGEL VILLAGES INC.
ALL RIGHTS RESERVED. PERMISSION TO REPRINT IN ITS ENTIRETY FOR NON-COMMERCIAL USE ONLY.
Prescribing Algorithms and Pharmacotherapy
Troubleshooting Guides
CONTRAINDICATIONS PRESENT?• Bilateral Renal Artery Stenosis
• Sever Aortic Stenosis• Angioedema/Allergy
ARE THE FOLLOWING SATISFIED?• Creatine Clearance > 30ml/min
• Potassium < 5.5 mmol/L• No symptomatic hypotension
CHECK-IN 7-14 DAYS• Creatine <30% increase• Potassium <5.5 mmol/L
• No symptomatic hypotension
If not at target increase dose in 2-4
weeksPrescribe ACEi
NO
YES
YES
1. Any reversible cause(s)? (See troubleshooting)2. If no reversible causes, reduce ACEi dose by 50%3. If no reversible causes on lowest ACEi dose or no
ACEi, then do not prescribe the ACEi
NO
NO RECHECK
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
DO NOT PRESCRIBE
YES
Using ACE Inhibitors (ACEi) for Heart Failure
Drug Starting DoseTitration
incrementIdeal Target Dose
Ramipril 1.25-2.5 mg od 2.5 mg 10 mg od or 5 mg bid
Lisinopril 2.5-5 mg od 5 mg od 30 mg od
Perindopril 2 mg od 2 mg 8 mg od
Enalapril 2.5-5 mg bid 5 mg od-bid 10 mg bid
CAUTIONif patient on
K+ supplements and/or ARB and/or
Spironolactone
CONTRAINDICATIONS PRESENT?• Bilateral Renal Artery Stenosis
• Sever Aortic Stenosis• Angioedema/Allergy
ARE THE FOLLOWING SATISFIED?• Creatine Clearance > 30ml/min
• Potassium < 5.5 mmol/L• No symptomatic hypotension
CHECK-IN 7-14 DAYS• Creatine <30% increase• Potassium <5.5 mmol/L
• No symptomatic hypotension
If not at target increase dose in 2-4
weeksPrescribe ARB
NO
YES
1. Any reversible cause(s)? (See troubleshooting)2. If no reversible causes, reduce ARB dose by 50%3. If no reversible causes on lowest ARB dose or no
ARB, then do not prescribe the ARB
NO
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
DO NOT PRESCRIBE
YES
Using Angiotensin Receptor Blockers (ARB) for Heart Failure
DrugStarting
DoseTitration
incrementIdeal Target
Dose
Candesartan 4 mg od 4-8 mg 32 mg od
Valsartan 40 mg od 40-80 mg 160 mg bid
CAUTIONif patient on
K+ supplements and/or ACEi and/or
Spironolactone
NO RECHECK
YES
CONTRAINDICATIONS PRESENT?• Bilateral Renal Artery Stenosis
• Sever Aortic Stenosis• Angioedema/Allergy
ARE THE FOLLOWING SATISFIED?• No concurrent use of ACEi or ARB• Creatine Clearance > 30ml/min
• Potassium < 5.5 mmol/L• No symptomatic hypotension
CHECK-IN 7-14 DAYS• Creatine <30% increase• Potassium <5.5 mmol/L
• No symptomatic hypotension
If not at target increase dose in 2-4
weeksPrescribe S/V
NO
YES
YES
1. If on ACEi, discontinue ACEi for > 36 hours2. If on ARB, discontinue ARB3. Any reversible cause(s)? (See troubleshooting)4. If no reversible causes, reduce S/V dose by 50%5. If no reversible causes on lowest S/V dose or no S/V, then do
not prescribe the S/V
NO
NO RECHECK
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
DO NOT PRESCRIBE
YES
Using Sacubitril/ Valsartan (S/V) in Heart Failure
Drug Starting DoseTitration
incrementIdeal Target
Dose
Sacubitril/Valsartan
24.3 mg/25.7 mg bid
48.6 mg/ 51.4 mg bid
97.3mg/ 102.8mg bid
CAUTION-stop previous
ACEi or ARB for >36 hours
-if patient on K+ supplements and/or
Spironolactone
CONTRAINDICATIONS PRESENT?• Symptomatic bradycardia• Severe reversible airway
obstruction• Allergy
ARE THE FOLLOWING SATISFIED?• No symptomatic hypotension
• SBP > 90mmHg and / or HR > 60/min• No current pulmonary congestion
Are the following ABSENT?• increased heart failure symptoms • fluid retention, weight gain (>2kg)
• Symptomatic hypotension or bradycardia (HR > 60/min)
If not at target then increase dose by 25-50% in 2-4 weeks
Prescribe ßB
NO
YES
YES
1. Any reversible cause(s)? (see troubleshooting)2. If no reversible cause, reduce βB dose by 50%3. If no reversible cause on lowest βB dose or no βB, then do not
prescribe the βB
NO
NO RECHECK
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
DO NOT PRESCRIBE
YES
Using Beta Blockers (ßB) for Heart Failure
Drug Starting DoseTitration
incrementIdeal Target Dose
Bisoprolol 1.25-2.5 mg od 2.5 mg 10 mg od
Carvedilol 3.125 mg bid 6.25-12.5 mg 25-50 mg bid
Metoprolol* 12.5-25 mg bid 12.5-25 mg 75-100 mg bid*Metoprolol tartrate, available in Canada, has not been validated for HF. Consider switching to bisoprolol.
*Switching from Metoprolol to Bisoprolol
Metoprolol 25 mg bid ≈ 2.5 mg od
Metoprolol 50 mg bid ≈ 5 mg od
Metoprolol 75 mg bid ≈ 7.5 mg od
Metoprolol 100 mg bid ≈ 10 mg od
ARE INDICATIONS PRESENT?• Optimal ACEi/ARB and ßB
• Persistent dyspnea with even mild exertion and LVEF <35%• Recent hospitalization and persistent dyspnea with moderate
exertion and either LVEF ≤30% or LVEF ≥35% and QRS duration >130ms• No intolerance
ARE THE FOLLOWING SATISFIED?• Creatine Clearance > 30ml/min
• Serum K+ < 5.2 mmol/L• Have potassium supplements and other potassium-sparing diuretics been stopped?
CHECK-IN 7-14 DAYS• Creatine <30% increase• Potassium <5.2 mmol/L
• No symptomatic hypotension
If not at target increase dose in
2-4 weeksPrescribe AA
YES
YES
YES
1. Any reversible cause(s)? (See troubleshooting)2. If no reversible causes, reduce AA dose by 50% if
already prescribed, or stop/do not prescribe
NO
NO RECHECK
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
DO NOT PRESCRIBE
NO
Using Aldosterone Antagonists (AA) for Heart Failure
Drug Starting Dose Target Dose
Spironolactone 12.5 mg od 50 mg od
Eplerenone 25 mg q 2 days 50 mg od
CAUTIONDiabetics have an increased risk of
hyperkalemia and worsening renal
function
ARE INDICATIONS PRESENT?• Optimal ACEi/ARB, ßB and AA
• LVEF <35%• Resting Heart Rate >70, sinus rhythm• Not taking verapamil or diltiazem
• Normal QT• No intolerance
ARE THE FOLLOWING PRESENT?• Symptomatic bradycardia
• Prolonged QT
CHECK RESTING HEART RATE WITHIN 7 DAYS AND MONTHLY THEREAFTER
• No symptomatic bradycardia or hypotension
If not at target increase dose in
2-4 weeksPrescribe Ivabradine (see table)
YES
YES
YES
1. Any reversible cause(s)? (See troubleshooting)2. If no reversible causes, reduce Ivabradine dose by
50% if already prescribed, or stop/do not prescribe
NO
NO RECHECK
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
DO NOT PRESCRIBE
NO
Using Ivabradine for Heart Failure
Drug Starting Dose Target Dose
Ivabradine 2.5 mg po bid 7.5 mg po bid
ARE INDICATIONS
PRESENT?• Optimal
ACEi/ARB, ßBand/or Aldosterone Antagonist
• Persistent dyspnea with minimal exertion
• Left ventricular ejection fraction <45%
• No intolerance
• Check digoxin level, electrolytes and creatinine
• Consider holding digoxin
• Consider starting dose based on adjacent table
• Cut-dose in half if on Amiodarone, Clarithromycin or Verapamil
YES
PRACTICE TIPS• Digoxin levels should be checked 8-12 hours
after last dose• Target level is 1ng/ml or 1.4 mmol/L• Symptoms of toxicity may be non-specific
and include anorexia, nausea, depression, anxiety or delirium
• No need for routine monitoring: check levels when symptoms present
For further details, please visit the Heart Failure Guidelines website: https://www.ccs.ca/en/guidelines/guidelines-library
OPTIMIZE OTHER DRUGS
FIRST
NO
Using Digoxin for Heart Failure Creatinine clearance (mL/min/1.73m2)
Lean Body Weight (kg)40 50 60 70 80 90 100
0102030405060708090
100
Monitor for digoxin toxicity if creatinine rises
(e.g., dehydrating illness)
Check Potassium given increase toxicity with hypokalemia
If K+ <3.5 mmol/L consider
potassium supplement or reduce digoxin
dosage and repeat lab work
31.25 mcg62.5 mcg
125.0 mcg187.5 mcg
Misiaszek et al, Can J Card, 2005
CAUTIONS
Issue• Resident
becomes dizzy
Pharmacological triggering event↑ Dose of ACEi↑ Dose of ARB↑ Dose of S/V↑ Dose of ß-BlockerAND/OR↑ Dose of Ivabradine
Pharmacotherapy Troubleshooting:
Possible Causes• Hypovolemia from inadequate fluid intake and/or excessive diuresis• Initial diuresis related to Sacubitril/Valsartan initiation• Concurrent use of non-first line cardiovascular medication (nitrates, vasodilator,
calcium-channel blocker)• Orthostatic hypotension related to psychotropic or anticholinergic drug (e.g.,
tricyclic, dopaminergic)• If bradycardia < 50, consider other rate/ rhythm altering drugs such as amiodarone
or digoxin, or heart block
Possible Solutions• Reduce diuretic and
monitor resident• Reduce dose or
eliminate potentially offending drug
• If heart block present, avoid ß-Blocker / Ivabradine and/or consider cardiology referral
Reassess Resident in 1 week
The resident is dizzy when ACEi, ARB, S/V, ß-Blocker or Ivabradine dose is increased
Issue• Creatinine rises
Pharmacological triggering event↑ Dose of ACEi↑ Dose of ARBAND/OR↑ Dose of S/V
Pharmacotherapy Troubleshooting:
Possible Causes• Hypovolemia from inadequate fluid intake and/or excessive diuresis• Initial diuresis related to Sacubitril/Valsartan initiation• Normal response to ACEi / ARB if increase is no greater than 30% from baseline• Concurrent use of Non-Steroidal Anti-Inflammatory Drug (NSAID)
Possible Solutions• Reduce diuretic and
monitor resident• Reduce dose or
eliminate potentially offending drug
Reassess Resident in 1 week
The creatinine rises after starting or increase ACEi, ARB or S/V dose
Issue• Creatinine
rises
Pharmacological triggering event↑ Dose of ACEi↑ Dose of ARB↑ Dose of S/VAND/OR↑ Dose of
spironolactone
Pharmacotherapy Troubleshooting:
Possible Causes• Worsening renal failure, especially among diabetic residents• Concurrent use of Non-Steroidal Anti-Inflammatory Drug (NSAID)• Resident prescribed potassium supplements
Possible Solutions• Reduce dose or eliminate potentially
offending drug• If no reversible cause found, and
resident is prescribed both an ACEI / ARB and an aldosterone antagonist, the preponderance of evidence suggests that aldosterone antagonist be discontinued first
Reassess Resident in 1 week
Hyperkalemia occurs when the ACEi, ARB, S/V, or spironolactone is increased
Issue• Cough
develops
Pharmacological trigger• Use of ACEi
Pharmacotherapy Troubleshooting:
Possible Causes• The resident has developed worsening pulmonary edema• The resident has developed an infectious process or has a post-
viral cough• The resident has developed an ACE-Inhibitor cough
Possible Solutions• Assess the resident for possible
pulmonary edema and treat with temporary increase in diuretics, the reassess
• If cough is TRULY intolerable and no obvious cause is found, stop the ACEi and consider and ARB. If cough persists with ARB, consider combination therapy with nitrates and hydralazine
Reassess Resident in 1 week
The resident develops a cough while on an ACEi